Application
Western blot analysis of anti-SFRS12 Pab in Jurkat (left) and SK-Br-3(left) cell line lysates (35ug/lane). SFRS12(arrow) was detected using the purified Pab (1:60 dilution).| Product Name | SFRS12 Antibody (C-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | SREK1; SFRS12; SRRP86; Splicing regulatory glutamine/lysine-rich protein 1; Serine/arginine-rich-splicing regulatory protein 86; Splicing factor, arginine/serine-rich 12; Splicing regulatory protein 508 |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WB |
| WB:1:100~500 |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | SFRS12 SRRP86 |
|---|---|
| Alternative Names | SREK1 SFRS12 SRRP86 Splicing regulatory glutamine/lysine-rich protein 1 Serine/arginine-rich-splicing regulatory protein 86 Splicing factor arginine/serine-rich 12 Splicing regulatory protein 508 |
| Molecular Weight(MW) | 59380 Da |
| Function | Participates in the regulation of alternative splicing by modulating the activity of other splice facors. Inhibits the splicing activity of SFRS1, SFRS2 and SFRS6. Augments the splicing activity of SFRS3 (By similarity) |
| Tissue Specificity | This SFRS12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 467~496 amino acids from the C-terminal region of human SFRS12. |
| Cellular Localization | Nucleus. |
| Entrez Gene | 140890 |
|---|
Application
Western blot analysis of anti-SFRS12 Pab in Jurkat (left) and SK-Br-3(left) cell line lysates (35ug/lane). SFRS12(arrow) was detected using the purified Pab (1:60 dilution).| Application Notes | WB:1:100~500 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles. |
| Storage Buffer | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS. |
